Genetic analysis of chromosome 22q11.2 markers in congenital heart disease-Reference-Cited by-同舟云学术

Genetic analysis of chromosome 22q11.2 markers in congenital heart disease

Published:2003 Issue:1 Volume:17 Page:28-35
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J. Clin. Lab. Anal.

Author:

Shi Yi-Ru,Hsieh Kai-Sheng,Wu Jer-Yuarn,Lee Cheng-Chun,Tsai Chang-Hai,Yu Ming-Tseng,Chang Jeng-Sheng,Tsai Fuu-Jen

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Reference13 articles.

1. Incidence of congenital heart disease: I. Postnatal incidence

2. Toward a Molecular Understanding of Congenital Heart Disease

3. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

4. Microdeletion 22q11 in complex cardiovascular malformations

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4. SNPs and real-time quantitative PCR method for constitutional allelic copy number determination, the VPREB1 marker case;BMC Medical Genetics;2011-05-05

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